Detalhe da pesquisa
1.
ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation.
Bioinformatics
; 40(4)2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38485690
2.
Clonal Hematopoiesis in Clinical and Experimental Heart Failure With Preserved Ejection Fraction.
Circulation
; 148(15): 1165-1178, 2023 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37681311
3.
High-dose AraC is essential for the treatment of ML-DS independent of postinduction MRD: results of the COG AAML1531 trial.
Blood
; 138(23): 2337-2346, 2021 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34320162
4.
Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia.
Nature
; 518(7540): 552-555, 2015 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25487151
5.
Humanized zebrafish enhance human hematopoietic stem cell survival and promote acute myeloid leukemia clonal diversity.
Haematologica
; 105(10): 2391-2399, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054079
6.
Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis.
J Med Genet
; 56(7): 427-433, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30803986
7.
Human definitive hematopoietic specification from pluripotent stem cells is regulated by mesodermal expression of CDX4.
Blood
; 129(22): 2988-2992, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28408465
8.
Clonal hematopoiesis and risk of acute myeloid leukemia.
Haematologica
; 104(12): 2410-2417, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31004019
9.
Special Therapy and Psychosocial Needs Identified in a Multidisciplinary Cancer Predisposition Syndrome Clinic.
J Pediatr Hematol Oncol
; 41(2): 133-136, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30028825
10.
Congenital neurodevelopmental anomalies in pediatric and young adult cancer.
Am J Med Genet A
; 173(10): 2670-2679, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28851129
11.
Nomenclature and definition in asymmetric regional body overgrowth.
Am J Med Genet A
; 173(7): 1735-1738, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28475229
12.
Parental Age and Risk of Infant Leukaemia: A Pooled Analysis.
Paediatr Perinat Epidemiol
; 31(6): 563-572, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940632
13.
Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.
BMC Geriatr
; 16: 80, 2016 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27060904
14.
Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection.
Nucleic Acids Res
; 42(10): e82, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24682816
15.
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia.
Am J Hum Genet
; 91(4): 685-93, 2012 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23040496
16.
Late toxicity of a novel allogeneic stem cell transplant using single fraction total body irradiation for hematologic malignancies in children.
J Pediatr Hematol Oncol
; 37(2): e94-e101, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25333837
17.
Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.
Hum Mol Genet
; 21(3): 647-55, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22042774
18.
Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.
J Pediatr
; 164(6): 1316-21.e3, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24657120
19.
Scope of hearing loss in Beckwith-Wiedemann syndrome and hemihypertrophy.
Am J Med Genet A
; 179(11): 2307-2310, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31339626
20.
A study to assess the efficacy of enasidenib and risk-adapted addition of azacitidine in newly diagnosed IDH2-mutant AML.
Blood Adv
; 8(2): 429-440, 2024 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37871309